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用于开发负载姜黄素和双氯芬酸的茶树油增强型微凝胶以治疗类风湿性关节炎的质量源于设计方法

QbD Approach for the Development of Tea Tree Oil-Enhanced Microemulgel Loaded with Curcumin and Diclofenac for Rheumatoid Arthritis Treatment.

作者信息

Pathak Shivam, Singh Ruhi, Hussain Afzal, Siddiqui Nasir Ali, Mittal Saurabh, Gupta Annie

机构信息

Department of Pharmaceutics, Amity Institute of Pharmacy, Amity University, Noida 201303, UP, India.

Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.

出版信息

Gels. 2024 Sep 30;10(10):634. doi: 10.3390/gels10100634.

Abstract

Rheumatoid arthritis, a chronic autoimmune disorder affecting millions worldwide each year, poses a significant threat due to its potential for progressive joint damage and debilitating pain if left untreated. Topical anti-inflammatory and analgesic treatments offer localized relief with reduced systemic side effects compared to conventional oral therapies, making them a promising option for managing rheumatoid arthritis. Therefore, the current study endeavored to formulate a microemulsion gel formulation loaded with diclofenac and curcumin for topical administration in the management of rheumatoid arthritis, utilizing Tea tree oil. The ratio of surfactant and cosurfactant was 4:1, assessed by pseudoternary phase diagram on the basis of the maximum emulsification region. The microemulsion underwent optimization using a Central Composite Rotatable Design (CCRD) with constraints of minimum particle size, polydispersity index, and maximum transmittance. The Curcufenac-T microemulsion had a particle size, polydispersity index (PDI), and transmittance of 151.82 ± 15.9 nm, 0.287 ± 0.021, and -5.78 ± 0.26 mV, respectively. DSC analyses confirmed the stability and compatibility of diclofenac and curcumin within the formulation. The microemulsion was changed into gel form by incorporating 1% carbopol-934. Skin permeation analysis revealed that the percentage of diclofenac permeated at 0.5 h from Curcufenac-T microemugel and the conventional gel was 12.1% and 3.9%, respectively, while at 12 h, the rates were 82.6% and 34.2%, respectively. In vitro permeability demonstrated significant potential for the effective delivery of diclofenac and curcumin to targeted sites, compared to conventional gel. Therefore, it was deduced that the Tea tree oil integrated diclofenac and curcumin microemulsion gel could enhance the effectiveness of diclofenac and serve as a promising vehicle for rheumatoid arthritis treatment.

摘要

类风湿性关节炎是一种每年影响全球数百万人的慢性自身免疫性疾病,如果不加以治疗,由于其可能导致进行性关节损伤和使人衰弱的疼痛,会构成重大威胁。与传统口服疗法相比,局部抗炎和镇痛治疗可提供局部缓解,且全身副作用减少,这使其成为治疗类风湿性关节炎的一个有前景的选择。因此,本研究致力于制备一种负载双氯芬酸和姜黄素的微乳凝胶制剂,用于类风湿性关节炎的局部给药,并使用了茶树油。表面活性剂和助表面活性剂的比例为4:1,通过基于最大乳化区域的伪三元相图进行评估。使用中心复合旋转设计(CCRD)对微乳进行优化,其约束条件为最小粒径、多分散指数和最大透光率。Curcufenac-T微乳的粒径、多分散指数(PDI)和透光率分别为151.82±15.9nm、0.287±0.021和-5.78±0.26mV。差示扫描量热法(DSC)分析证实了双氯芬酸和姜黄素在制剂中的稳定性和相容性。通过加入1%的卡波姆-934将微乳转变为凝胶形式。皮肤渗透分析表明,Curcufenac-T微乳凝胶和传统凝胶在0.5小时时双氯芬酸的渗透百分比分别为12.1%和3.9%,而在12小时时,这一比率分别为82.6%和34.2%。体外渗透性表明,与传统凝胶相比,双氯芬酸和姜黄素有效递送至靶部位具有显著潜力。因此,可以推断,含有茶树油的双氯芬酸和姜黄素微乳凝胶可以提高双氯芬酸的有效性,并成为治疗类风湿性关节炎的一种有前景的载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae6/11507205/a2e9f54390c7/gels-10-00634-g001.jpg

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